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首页> 外文期刊>European Polymer Journal >Tough biohydrogels with interpenetrating network structure by bienzymatic crosslinking approach
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Tough biohydrogels with interpenetrating network structure by bienzymatic crosslinking approach

机译:通过双酶交联方法具有互穿网络结构的坚韧生物水凝胶

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摘要

Enzymatically crosslinked biohydrogels have increasingly attracted attention mainly due to the mildness of this type of reaction. However, their mechanical strength is usually so weak that their applications are limited in the field of medicine. In order to improve their mechanical properties and degradation resistance, bienzymatic crosslinking approach was utilized to prepare biohydrogels of gelatin and chitosan with an interpenetrating polymer network (IPN) structure in this report. First of all, chitosan was grafted with phloretic acid (chitosan-PA) used as a substrate of horseradish peroxidase (HRP). After that, the gelation process of gelatin/chitosan-PA IPN hydrogels was monitored by a rheometer. The results indicated the formation of dual networks: one gelatin network crosslinked by transglutaminase (TG) and another chitosan-PA network crosslinked by HRP in the presence of a low concentration of H2O2. In addition, the mechanical performances of the hydrogels were measured by a universal testing machine. It was found that the mechanical properties of the IPN gels were significantly improved compared with gelatin hydrogel crosslinked by TG. Moreover, the swelling ratio, degradation behavior, and cytocompatibility of the IPN hydrogels were investigated in detail. The preliminary biological evaluation indicated that the IPN hydrogels can support L929 cell adhesion and proliferation. Overall, the gelatin/chitosan IPN hydrogels prepared by bienzymatic crosslinking approach have excellent biocompatibility and mechanical properties. Therefore, dual enzyme-mediated crosslinking of natural polymer hydrogels is promising for the development of tissue engineering scaffolds and wound dressing. (C) 2015 Elsevier Ltd. All rights reserved.
机译:酶促交联的生物水凝胶越来越引起人们的关注,这主要是由于这种反应的温和性。但是,它们的机械强度通常很弱,以致其在医学领域的应用受到限制。为了提高它们的机械性能和抗降解性,在本报告中,利用双酶交联方法制备了具有互穿聚合物网络(IPN)结构的明胶和壳聚糖生物水凝胶。首先,将壳聚糖与用作辣根过氧化物酶(HRP)底物的苯甲酸(壳聚糖-PA)接枝。之后,通过流变仪监测明胶/壳聚糖-PA IPN水凝胶的凝胶化过程。结果表明形成了双重网络:在低浓度的H2O2存在下,一个明胶网络通过转谷氨酰胺酶(TG)交联,另一个壳聚糖-PA网络通过HRP交联。另外,水凝胶的机械性能通过通用测试机测量。发现与通过TG交联的明胶水凝胶相比,IPN凝胶的机械性能得到显着改善。此外,详细研究了IPN水凝胶的溶胀率,降解行为和细胞相容性。初步生物学评估表明,IPN水凝胶可支持L929细胞粘附和增殖。总体而言,通过双酶交联方法制备的明胶/壳聚糖IPN水凝胶具有出色的生物相容性和机械性能。因此,天然聚合物水凝胶的双酶介导交联有望用于组织工程支架和伤口敷料的开发。 (C)2015 Elsevier Ltd.保留所有权利。

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